The Vespiary

The Hive => Novel Discourse => Topic started by: slothrop on December 17, 2002, 08:58:00 AM

Title: Benzyl alcohols to Benzaldehydes
Post by: slothrop on December 17, 2002, 08:58:00 AM

From Synlett 2002, 12, pp2041-42,
A Novel and Efficient Oxidation of Benzyl Alcohols to Benzaldehydes with DMSO Catalyzed by Acids

Typical procedure: A mixture of 557 mg of benzyl alcohol, 0.15 mL of HBr (48 %) and 5 mL of DMSO was stirred in an oil bath at 100°C. TLC (petroleum ether/diethyl ether, 1:1) was used to indicate the completion of the reaction (3 h). To the reaction mixture were added 5 mL brine followed by extraction with 30 mL of diethyl ether. The ether layer was washed with brine (5 mL x 4). Evaporation of the ether and subsequent buld to buld distillation produced 530 mg of benzaldehyde in 95 % yield.

//Tyrone Slothrop
Title: Re: Benzaldehydes
Post by: java on December 17, 2002, 01:33:00 PM
Good find, ........congratulations!
Title: Complete article
Post by: Rhodium on December 17, 2002, 02:55:00 PM

https://www.thevespiary.org/rhodium/Rhodium/chemistry/benzaldehydes.dmso.html (https://www.thevespiary.org/rhodium/Rhodium/chemistry/benzaldehydes.dmso.html)

Title: whoops :-)
Post by: slothrop on December 17, 2002, 03:06:00 PM
Ops, sorry for being redundant.

//Tyrone Slothrop